Asymmetric Synthesis with the Enzyme Coprinus Peroxidase: Kinetic

Novel Model Sulfur Compounds as Mechanistic Probes for Enzymatic and Biomimetic Oxidations. Alicia B. Pe ory , Juan E. Arg ello , Marcelo Puiatti...
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J. Org. Chem. 1999, 64, 4834-4839

Asymmetric Synthesis with the Enzyme Coprinus Peroxidase: Kinetic Resolution of Chiral Hydroperoxides and Enantioselective Sulfoxidation Waldemar Adam,* Cordula Mock-Knoblauch, and Chantu R. Saha-Mo¨ller Institut fu¨ r Organische Chemie der Universita¨ t Wu¨ rzburg, Am Hubland, D-97074 Wu¨ rzburg, Germany Received February 2, 1999

The enzyme Coprinus peroxidase (CiP) was employed for the kinetic resolution of racemic hydroperoxides 1 and the asymmetric sulfoxidation of prochiral sulfides 4. Eleven hydroperoxides 1a-k were reduced by CiP and guaiacol as reductant under conditions of kinetic resolution with enantioselectivities of up to >98% for the (S)-hydroperoxide 1 and 90% for the (R)-alcohol 2. In the absence of a reductant, the hydroperoxide 1a afforded with CiP enantiomerically enriched hydroperoxide 1a (ee up to 54%) and alcohol 2a (ee up to 40%), as well as ketone 3a (which is also formed simultaneously in all other reactions) and molecular oxygen. Catalase activity was established for CiP with hydrogen peroxide. When aryl alkyl sulfides 4 were used as oxygen acceptors, three products, sulfoxides 5, alcohols 2, and hydroperoxides 1, were obtained, all in enantiomerically enriched form. The highest ee value (89%) was achieved for the sulfoxide derived from naphthyl methyl sulfide (4f). Thus, CiP may be utilized for the asymmetric synthesis of optically active hydroperoxides 1, alcohols 2, and sulfoxides 5. Introduction In recent years, enzymes have increasingly been used for the synthesis of optically active compounds.1 In particular, peroxidases have proven to be versatile biocatalysts for a number of redox transformations.2 Among the best-known peroxidases is chloroperoxidase from Caldariomyces fumago (CPO), which, for example, catalyzes enantioselective epoxidations,3 sulfoxidations,4 and benzylic hydroxylations.5 Also, horseradish peroxidase (HRP) has been intensively studied for the kinetic resolution of hydroperoxides.6 In many of these reactions, good to excellent enantioselectivities have been obtained; unfortunately, this selectivity advantage comes at the dear price of limited scope of substrate acceptance by the * To whom correspondence should be addressed. E-mail: adam@ chemie.uni-wuerzburg.de. Fax: +49-931-8884756. (1) (a) Enzymes in Synthetic Organic Chemistry; Wong, C. H., Whitesides, G. M., Eds.; Pergamon Press: Oxford, 1994. (b) Drautz, K.; Waldmann, H. Enzyme Catalysis in Organic Synthesis; VCH: Weinheim, 1995. (2) (a) van Deurzen, M. P. J.; van Rantwijk, F.; Sheldon, R. A. Tetrahedron 1997, 39, 13183-13220. (b) Adam, W.; Lazarus, M.; SahaMo¨ller, C. R.; Weichold, O.; Hoch, U.; Ha¨ring, D.; Schreier, P. In Advances in Biochemical Engineering/Biotechnology; Faber, K., Ed.; Springer-Verlag: Heidelberg, 1999; Vol. 63, p 73. (3) (a) Colonna, S.; Gaggero, N.; Casella, L.; Carrea, G.; Pasta, P. Tetrahedron: Asymmetry 1993, 4, 1325-1330. (b) Allain, E. J.; Hager, L. P.; Deng, L.; Jacobsen, E. N. J. Am. Chem. Soc. 1993, 115, 44154416. (c) Lakner, F. J.; Hager, L. P. J. Org. Chem. 1996, 61, 39233925. (d) Dexter, A. F.; Lakner, F. J.; Campbell, R. A.; Hager, L. P. J. Am. Chem. Soc. 1995, 117, 6412-6413. (4) (a) Colonna, S.; Gaggero, N.; Casella, L.; Carrea, G.; Pasta, P. Tetrahedron: Asymmetry 1992, 3, 95-106. (b) Fu, H.; Kondo, H.; Ichikawa, Y.; Look, G. C.; Wong, C. H. J. Org. Chem. 1992, 57, 72657270. (c) van Deurzen, M. P. J.; Remkes, I. J.; van Rantwijk, F.; Sheldon, R. A. J. Mol. Catal. A: Chemical 1997, 117, 329-337. (5) (a) Miller, V. P.; Tschirret-Guth, R. A.; Ortiz de Montellano, P. R. Arch. Biochem. Biophys. 1995, 319, 333. (b) Zaks, A.; Dodds, D. R. J. Am. Chem. Soc. 1995, 117, 10419-10424. (6) (a) Adam, W.; Hoch, U.; Lazarus, M.; Saha-Mo¨ller, C. R.; Schreier, P. J. Am. Chem. Soc. 1995, 117, 11898-11901. (b) Adam, W.; Hoch, U.; Humpf, H.-U.; Saha-Mo¨ller, C. R.; Schreier, P. J. Chem. Soc., Chem. Commun. 1996, 2701-2702. (c) Hoch, U.; Adam, W.; Fell, R. T.; Saha-Mo¨ller, C. R.; Schreier, P. J. Mol. Catal. A, Chem. 1997, 117, 321-328.

enzyme. Moreover, many enzymes accept only one of the substrate enantiomers, such that the other antipode is usually inaccessible. However, recently we have discovered that the microorganism Bacillus subtilis possesses peroxidase activity in which the opposite enantiomer of the hydroperoxide is recognized as by the horseradish peroxidase.7 This favorable finding encouraged us to screen other peroxidases for their selectivity and substrate acceptance to enable the biocatalytic synthesis of both optically active enantiomers for a wide variety of functionalized substrates. The Coprinus peroxidase (CiP), which has been isolated from the basidiomycete Coprinus cinereus,8 is known from its X-ray crystal structure9 to have a rather large substrate opening and should, therefore, be a favorable candidate to accept a broad range of substrates, also sterically encumbered ones. We have applied the enzyme Coprinus peroxidase for the kinetic resolution of racemic hydroperoxides and the enantioselective oxidation of prochiral sulfides and report herein our results. Results and Discussion Kinetic Resolution of Hydroperoxides. In our efforts to provide optically enriched hydroperoxides, which may be used as oxidants in asymmetric synthesis,10 we have shown that the kinetic resolution of racemic hydroperoxides with horseradish peroxidase (HRP) constitutes a useful way to achieve this goal.6 Unfortunately, (7) Adam, W.; Boss, B.; Harmsen, D.; Lukacs, Z.; Saha-Mo¨ller, C. R.; Schreier, P. J. Org. Chem. 1998, 63, 7598-7599. (8) (a) Shinmen, Y.; Asami, S.; Amachi, T.; Shimizu, S.; Yamada, H. Agric. Biol. Chem. 1986, 50, 247-249. (b) Morita, Y.; Yamashita, H.; Mikami, B.; Iwamoto, H.; Aibara, S.; Terada, M.; Minami, J. J. Biochem. 1988, 103, 693-699. (9) (a) Petersen, J. F. W.; Kadziola, A.; Larsen, S. FEBS Lett. 1994, 339, 291-296. (b) Abelskov, A. K.; Smith, A. T.; Rasmussen, C. B.; Dunford, H. B.; Welinder, K. G. Biochemistry 1997, 36, 9453-9463. (10) (a) Adam, W.; Korb, M. N.; Roschmann, K. J.; Saha-Mo¨ller, C. R. J. Org. Chem. 1998, 63, 3423-3428. (b) Adam, W.; Korb, M. N. Tetrahedron: Asymmetry 1997, 8, 1131-1142.

10.1021/jo990201p CCC: $18.00 © 1999 American Chemical Society Published on Web 06/06/1999

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Table 1. CiP-Catalyzed Kinetic Resolution of Hydroperoxides 1 in the Presence of Guaiacola

HRP does not catalyze the kinetic resolution of sterically hindered and, particularly, tertiary hydroperoxides.6a For this purpose, we have employed CiP, since, as already mentioned, its X-ray crystal structure exposed a rather large opening for substrate entry.9a To establish the catalytic efficiency and the substrate selectivity of CiP, we examined a series of sterically and electronically varied racemic hydroperoxides 1, with emphasis on those substrates that are not satisfactorily converted by HRP. The results (Table 1) show that the hydroperoxide structure dramatically influences the enantioselectivity and the enantiomeric preference of the CiP enzyme. An increase of the chain length of the alkyl group in the case of the alkyl aryl hydroperoxide leads to a drastic reduction of the reactivity and selectivity. Whereas for the hydroperoxides 1a-c with a methyl group good to excellent enantioselectivities were obtained at low enzyme concentration in relatively short reaction times (entries 1-3), for the substrates with sterically more demanding alkyl groups, e.g., 1d-f, low or even no selectivity was observed (entries 4-6). By comparison,

the variation of the aryl group does bring about significant changes in the efficiency of enantiomeric control, as exemplified by the hydroperoxides 1a-c (entries 1-3), but not as pronounced as does the alkyl group in the derivatives 1d-f (entries 4-6). Interestingly, the enzyme CiP shows better reactivity and selectivity toward the cyclic hydroperoxide 1g than toward the corresponding acyclic hydroperoxide 1d (entries 7 and 4, respectively). Apparently, the conformationally more rigid cyclic structure fits well into the enzyme pocket. Sterically more demanding hydroperoxides such as 1i,j show almost no conversion to the corresponding alcohols even at large enzyme concentrations and long reaction times (entries 9 and 10). Instead, the transformation of the hydroperoxide to the corresponding ketone was observed. Considerable amounts of ketone were also obtained for substrates 1d-f with alkyl groups larger than methyl (entries 4-6). Unfortunate for our purposes, the tertiary hydroperoxide 1k (entry 11) was only ineffectively converted to the corresponding alcohol 2k.

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Table 2. CiP-Catalyzed Sulfoxidation with Racemic (1-Phenyl)ethyl Hydroperoxidea

Interestingly, a β-hydroxy group in the hydroperoxide 1h does not decrease the reactivity and selectivity as much as prolongation of the alkyl chain in the ethyl derivative 1d (entries 8 and 4, respectively). Thus, although steric effects play an important role, electronic factors are as well significant for enantiodifferentiation by the enzyme. In all the hydroperoxides in Table 1, CiP preferentially accepts the R enantiomer as substrate with concurrent formation of the (R)-alcohol, while the (S)-hydroperoxide is left behind (entries 1-6, 8). An exception is the cyclic hydroperoxide 1g, for which the S enantiomer is converted to the alcohol and the (R)-hydroperoxide remains (entry 7).11 Evidently, the structural arrangement of the CiP enzyme pocket, which preferentially accommodates the short alkyl chain in the hydroperoxides 1a-d, also accepts well the larger but flat phenyl group. These results clearly establish the limitations of CiPcatalyzed kinetic resolution of hydroperoxides. Like HRP, CiP also shows very good enantioselectivity for aryl alkyl (11) It should be noted that for the hydroxy-functionalized hydroperoxide 1h a change in the sequence priority applies, and thus, the stereoselection is the same.

hydroperoxides with short alkyl chains. Sterically more encumbered and particularly tertiary hydroperoxides, however, are not or only unselectively reduced. The sense of the enantioselectivity is also the same for CiP as for HRP, except for the indanyl hydroperoxide 1g. The larger substrate opening of the CiP enzyme, which had prompted us to examine sterically more demanding hydroperoxides, has not held up to our expectations. Enantioselective Sulfoxidation. Peroxidases also possess the ability to catalyze oxygen-transfer reactions. Whereas CPO also catalyzes epoxidations,3 most other peroxidases only oxidize sulfides.4,12 We have investigated herein the oxygen-transfer propensity of CiP by using the enantioselective sulfoxidation as the model reaction. For this purpose, seven electronically and sterically varied prochiral sulfides 4 were oxidized by CiP (Table 2). As oxidant, racemic (1-phenyl)ethyl hydroperoxide (1a) was used, which had been shown to be best in the CiP(12) (a) Colonna, S.; Gaggero, N.; Carrea, G.; Pasta, P. J. Chem. Soc., Chem. Commun. 1992, 357-358. (b) Ozaki, S.-I.; Ortiz de Montellano, P. R. J. Am. Chem. Soc. 1994, 116, 4487-4488. (c) Ozaki, S.-I.; Ortiz de Montellano, P. R. J. Am. Chem. Soc. 1995, 117, 7056-7064. (d) Ortiz de Montellano, P. R. Annu. Rev. Pharmacol. Toxicol. 1992, 32, 89107.

Asymmetric Synthesis with Coprinus Peroxidase

catalyzed kinetic resolution experiments. If successful, three optically active compounds would be prepared simultaneously, namely, the sulfoxide 5, the alcohol 2, and the hydroperoxide 1. That this is feasible was nicely demonstrated by Wong et al. for the CPO enzyme.4b In a preliminary experiment, the same reaction conditions were used for the enantioselective sulfoxidation of methyl phenyl sulfide (4a) as for the kinetic resolution of hydroperoxides (Table 2, entry 1). At complete sulfide conversion, only racemic sulfoxide 5a was obtained. A control experiment without enzyme showed that under these conditions the sulfide was almost completely oxidized by the hydroperoxide (entry 2). This undesirable direct chemical sulfoxidation was minimized by employing low sulfide concentrations and a higher amount of enzyme (entry 3). Under these conditions, the CiPcatalyzed enantioselective sulfoxidation of methyl phenyl sulfide (4a) was achieved in moderate (39%) enantioselectivities for the sulfoxide 5a. In the case of the alkyl aryl sulfides 4b and 4c, in which the phenyl rings are substituted with para electron-donating substituents, among the best (79%) enantioselectivities were obtained for the (S)-(-)-sulfoxides 5b and 5c (entries 4 and 5). Most pleasingly, high ee values were also found for the (S)-(-)-hydroperoxide 1a (>95%) and for the (R)-(+)alcohol 2a (ca. 65%). In contrast, methyl p-nitrophenyl sulfide (4d) was not converted at all to the corresponding sulfoxide (entry 6), which may be ascribed to the deactivation of the sulfide toward oxidation due to the electron-withdrawing para substituent.4a,c As was the case for the kinetic resolution of the hydroperoxides 1, prolongation of the alkyl chain in the ethyl tosyl sulfide (4e) strongly reduced the reactivity and selectivity (entry 7). Benzyl methyl sulfide (4g) also proved to be a poor substrate for the CiP-catalyzed sulfoxidation (entry 9). Only low conversion and almost no enantioselectivity were observed. The best substrate was methyl naphthyl sulfide (4f), which was oxidized with the highest ee value of 89% (entry 8). The large steric difference between the naphthyl and the methyl groups in this prochiral sulfide is clearly advantageous for effective stereodifferentiation. In all cases, the (S)-sulfoxide was formed, in contrast to the reactions catalyzed by CPO, which displays enantioselectivities up to >98% for a number of aryl sulfides4c in favor of the (R)-sulfoxide.4 This makes the enzyme CiP a valuable native biocatalyst for the asymmetric synthesis of sulfoxides since the “opposite” enantiomer is made available. However, compared to CPO, the turnover number of CiP in the asymmetric sulfoxidation is lower and the substrate acceptance is more limited. The major advantage of the CiP-catalyzed sulfoxidation is that the hydroperoxide, sulfide, and enzyme are all mixed at once, while with CPO the cumbersome slow continuous addition of the oxygen donor is required.4 Thus, the present CiP-catalyzed sulfoxidation contributes a biocatalytic process for the synthesis of selected (S) sulfoxides, which should serve as valuable synthons for the preparation of natural products and as powerful stereodirecting groups in asymmetric synthesis.13 Catalase Activity and Ketone Formation from the Alkyl Hydroperoxides. Unfortunately, up to 40% of the (13) (a) Mata, E. G. Phosphorus, Sulfur Silicon 1996, 117, 231286. (b) Kagan, H. B.; Rebiere, F.; Samuel, O. Phosphorus, Sulfur Silicon 1991, 58, 89-110. (c) Carren˜o, M. C. Chem. Rev. 1995, 95, 1717-1760.

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Figure 1. (a) CiP-catalyzed disproportionation of hydrogen peroxide [UV absorption at 240 nm, 200 µmol of H2O2, 60 µmol of CiP in 3 mL of 1 M phosphate buffer (pH 7.0)]. (b) Oxygengas evolution during the CiP-catalyzed disproportionation of (1-phenyl)ethyl hydroperoxide (1a) [18 µmol 1a, 300 nmol CiP in 2 mL of 1 M phosphate buffer (pH 7.0)].

hydroperoxide 1a used in the sulfoxidation reactions is converted to the corresponding ketone 3a, whereby the oxidation of the sulfide to sulfoxide is substantially reduced. When, however, 1 equiv of hydrogen peroxide was used as oxidant instead of hydroperoxide 1a in the CiP-catalyzed sulfoxidation, no conversion of the sulfide was observed although the H2O2 was completely consumed.14 This prompted us to test whether the peroxidase CiP also possesses catalase activity, i.e., catalyzes the disproportionation of hydrogen peroxide to water and molecular oxygen. Indeed, the UV absorption of hydrogen peroxide at 240 nm decreased upon addition of CiP to a solution of hydrogen peroxide in phosphate buffer (pH 7.0), as displayed in Figure 1a. Clearly, with hydrogen peroxide as oxygen source, the resulting compound I of the enzyme prefers to react with another molecule of hydrogen peroxide to produce O2 through paths A and D rather than oxidize the sulfide to its sulfoxide along paths A and C in Scheme 1. (14) While this manuscript was in preparation, the following paper appeared: Tuynman, A.; Vink, M. K. S.; Dekker, H. L.; Schoemaker, H. E.; Wever, R. Eur. J. Biochem. 1998, 258, 906-913. The authors describe the CiP-catalyzed formation of (S)-methyl phenyl sulfoxide with a yield of 84% and an ee of 73%, when an excess of H2O2 is added slowly, as catalase activity accounts for 85% of the H2O2 consumption.

4838 J. Org. Chem., Vol. 64, No. 13, 1999 Scheme 1. Catalytic Cycles of Coprinus Peroxidase (CiP): Peroxidase (A + B), Catalase (A + D), and Monooxygenase (A + C) Activity

In contrast, with the hydroperoxide 1a as oxygen source, some asymmetric sulfoxidation takes place (Table 2); however, when CiP was allowed to react with hydroperoxide 1a in the absence of a reductant, oxygen-gas evolution, which was monitored by means of an oxygen electrode, was observed (Figure 1b). To understand the origin of the oxygen evolution, a careful product study of the reaction between hydroperoxide 1a and CiP was conducted (Table 3, entry 1). Mechanistically significant, in addition to alcohol 2a substantial amounts of ketone 3a were also observed, even when the isolated pure enzyme was employed (entry 2), accompanied by oygen-gas release. The ratio of alcohol to ketone was 1:1, independent of the extent of conversion (entry 3). Also the sterically more hindered hydroperoxide 1f gave the corresponding ketone 3f in addition to the alcohol 2f, but in an alcohol-to-ketone ratio of about 1:4 (entry 4). The appreciable ee values for the hydroperoxide 1a and alcohol 2a (entries 1-3) show clearly that an enzymatic stereodifferentiating process is involved. In this context, Hager et al. were the first who reported the formation of molecular oxygen in the reaction between CPO and ethyl hydroperoxide.15 They attributed the liberation of oxygen to the catalase activity of CPO toward alkyl hydroperoxides, as has been documented for hydrogen peroxide.16 However, this seems questionable because early work claims that catalase itself does not catalyze the disproportionation of alkyl hydroperoxides into alcohol and O2.17 Also acetaldehyde was observed, presumed to be formed by CPO-catalyzed two(15) Thomas, J. A.; Morris, D. R.; Hager, L. P. J. Biol. Chem. 1970, 245, 3129-3134. (16) (a) Hager, L. P.; Hollenberg, P. F.; Rand-Meir, T.; Chiang, R.; Doubek, D. Ann. N. Y. Acad. Sci. 1975, 244, 80-93. (b) Araiso, T.; Rutter, R.; Palcic, M. M.; Hager, L. P.; Dunford, H. B. Can. J. Biochem. 1981, 59, 233-236. (17) Chance, B. J. Biol. Chem. 1949, 180, 947-959.

Adam et al.

electron oxidation of the ethanol, which in turn derives from the ethyl hydroperoxide through reduction.15 This, indeed, is the known mechanism for the reaction of alkyl hydroperoxides with catalases18 and has also been reported to work enantioselectively with soybean lipoxygenase (SBLO).19 More recently, the mechanism of oxygen production was clarified. EPR-spectral evidence demonstrated the generation of peroxyl radicals in the reaction of peroxidases with hydroperoxides.20 Moreover, it was shown that about 12% of the released oxygen is electronically excited singlet oxygen.21 It was, thus, suggested that the peroxyl radicals, generated by enzymatic one-electron oxidation of the hydroperoxide, disproportionate according to the Russell mechanism22 into ketone, alcohol, and O2 in a ratio of 1:1:1 (Scheme 2). This reaction, however, only constitutes a minor path for the formation of acetaldehyde; the major one involves the oxidation of ethanol, as suggested by Hager.21 In our experiments with CiP, however, the possibility that the ketone 3a is formed by the oxidation of the alcohol 2a15,21,23 was discounted by the fact that the alcohol resisted CiP-catalyzed treatment with hydrogen peroxide or alkyl hydroperoxides 1b and 1e as oxygen sources. Thus, a plausible pathway for the formation of O2 and ketone (Scheme 2) is through the intervention of peroxyl radicals, enzymatically generated by the CiP, which disproportionate into alcohol 2, ketone 3, and O2 in a 1:1:1 ratio according to the Russell mechanism.22 However, if the overall reaction in Scheme 2 were the only pathway for the ketone formation, an alcohol/ketone ratio of 2:1 would be expected, i.e., 1 mol of alcohol results from the reduction of the hydroperoxide for the formation of compound I and another mol from the enzymatically produced peroxyl radicals through the Russell cleavage, together with 1 mol of ketone. Instead, an alcohol/ketone ratio of 1:1 was obtained for hydroperoxide 1a and even 1:4 for 1f. This implicates that, besides the Russell cleavage, some of the ketone must be formed from the hydroperoxide by an additional pathway. That this pathway is also an enzyme-catalyzed reaction and not merely base-catalyzed dehydration of the hydroperoxide (Kornblum-DeLaMare reaction24), has been confirmed by means of a control experiment, in which each hydroperoxide 1a and 1f was stirred under the usual reaction conditions [phosphate buffer (pH 7.0)] without the CiP enzyme; after 4 h (1a) and even 3 days (1f), the hydroperoxides were recovered unchanged. With the experimental data on hand, it is difficult to suggest which additional enzymatic pathway is responsible for the ketone formation. What may be stated definitely (see control experiment) is that the ketone is (18) Fita, I.; Rossmann, M. G. J. Mol. Biol. 1985, 185, 21-37. (19) Scettri, A.; Bonadies, F.; Lattanzi, A.; Palombi, L.; Pesci, S. Tetrahedron 1997, 53, 17139-17150. (20) (a) Davies, M. J. Biochim. Biophys. Acta 1988, 964, 28-35. (b) Chamulitrat, W.; Takahashi, N.; Mason, R. P. J. Biol. Chem. 1989, 264, 7889-7899. (21) Hall, R. D.; Chamulitrat, W.; Takahashi, N.; Chignell, C. F.; Mason, R. P. J. Biol. Chem. 1989, 264, 7900-7906. (22) (a) Russell, G. A. J. Am. Chem. Soc. 1957, 79, 3871-3877. (b) Horward, J. A.; Ingold, K. U. J. Am. Chem. Soc. 1968, 90, 1058-1059. (c) Nakano, M.; Takayama, K.; Shimizu, Y.; Tsuji, Y.; Inaba, H.; Migita, T. J. Am. Chem. Soc. 1976, 98, 1974-1975. (23) Geigert, J.; Dalietos, D. J.; Neidleman, S. L.; Lee, T. D.; Wadsworth, J. Biochem. Biophys. Res. Commun. 1983, 114, 11041108. (24) Kornblum, N.; DeLaMare, H. E. J. Am. Chem. Soc. 1951, 73, 880-881.

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Table 3. CiP-Catalyzed Decomposition of the Hydroperoxides 1 to Alcohols 2 and Ketones 3 in the Absence of Guaiacola

Scheme 2. Formation of Peroxyl Radicals by CiP-Catalyzed Oxidation of Hydroperoxides and Their Disproportionation to Ketone, Alcohol, and Molecular Oxygen (Russell Mechanism)

not formed by enzymatic oxidation of the alcohol, which is known for the CPO-catalyzed transformation of primary alcohols to aldehydes.15,23 Be this as it may, the enantioselective degradation of a chiral secondary hydroperoxide by a peroxidase in the absence of a reductant is unprecedented for such enzymes. In summary, we have demonstrated that, besides the usual peroxidase activity, CiP also acts as catalase

toward hydrogen peroxide. In its reaction cycle (Scheme 2), CiP uses alkyl hydroperoxides, on one hand, as substrates for the formation of compound I and, on the other hand, for the generation of peroxyl radicals by the reduction of compound I back to the native enzyme through compound II. The peroxidase activity of CiP may be used for the synthesis of optically active products by the kinetic resolution of hydroperoxides and enantioselective sulfoxidation, which provides (S)-(-)-hydroperoxides, (R)-(+)-alcohols, and (S)-(-)-sulfoxides in enantiomeric excess up to >90%. Clearly, the CiP peroxidase constitutes a promising enzyme for large-scale synthetic applications.

Acknowledgment. We thank NovoNordisk for the generous gift of CiP samples and the Deutsche Forschungsgemeinschaft (SFB-347 “Selektive Reaktionen Metall-aktivierter Moleku¨le”) and the Fonds der Chemischen Industrie for financial support. We also thank Prof. P. Schreier, University of Wu¨rzburg, for help with the oxygen measurements. Supporting Information Available: Experimental procedures with the tabulated HPLC conditions for the determination of the ee values of the hydroperoxides 1, alcohols 2, and sulfoxides 5 on chiral columns. This material is available free of charge via the Internet at http://pubs.acs.org. JO990201P